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Gaps in the sequences were treated as missing data.
Gaps in the sequences were treated as missing data and all characters were equally weighted.
Progressively, additional sequences were treated manually.
Gaps in the alignments of the sequences were treated as missing data.
Sequences were treated gene independent, mitochondrial versus nuclear partition and a total concatenated matrix.
Diploid sequences were treated using Haplotyper [ 48] to produce two haploid sequences per individual.
Similar(39)
For instance, the problem of estimating the MIMO channel covariance, based on limited amounts of training sequences, is treated in [47].
RNA-seq data can also be used to detect tissue-specific editing if the read sequences are treated as EST/mRNA sequences.
Repeat-masked sequences are treated equally for all methods.
The long-fragment indel of Chs sequences was treated as a one-mutation step and recoded.
This type of sequences is treated separately from the obvious functional OR genes or pseudogenes (see below).
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